FORMULATION AND EVALUATION OF CARVEDILOL SUBLINGUAL TABLET

被引:0
|
作者
Siji, C. [1 ]
Augusthy, Ann Rose [2 ]
Vipin, K. V. [2 ]
机构
[1] Natl Coll Pharm, Manassery, Kerala, India
[2] Acad Pharmaceut Sci, Pariyaram, Kerala, India
来源
关键词
Carvedilol; Sublingual tablet; Super disintegrants; Bioavailability;
D O I
10.5281/zenodo.1185156
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Carvedilol is an oral antihypertensive agent. Due to its poor water solubility it posses problems of variable bioavailability and bioequivalence. In the present work an attempt was done to develop sublingual tablets of carvedilol using different superdisintegrants like crosscarmellose sodium, crosspovidone and sodium starch glycolate in different ratios. As carvedilol is a poor soluble drug the solubility was enhanced by solid dispersion method. Tablets were prepared by direct compression technique. Prepared tablets were evaluated for thickness, uniformity of weight, hardness, friability, wetting time, in-vitro disintegration time, drug content and in vitro drug release. All the formulations were evaluated for the characteristics of sublingual tablets mainly in terms of. disintegration time and dissolution studies. Out of the 7 formulation, formulation F7 shows the maximum drug release. The formulation F7 consist of super disintegrant crosscarmellose sodium 5% and drug polymer in the ratio 1:4.From the literature it was evident that drug release was increased with increase in concentration of the polymer. So the formulation F7 was optimized as the best formulation.
引用
收藏
页码:1043 / 1050
页数:8
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